Search Results (4)

Since the 1960s, theorists have claimed that the electroweak force, which unifies parity-conserving electromagnetic and parity-violating weak nuclear forces, induces tiny parity-violating energy differences (10⁻¹⁰–10⁻²¹ eV) between mirror-image molecules. This study reports the dual mirror-symmetry-breaking and second-order phase transition characteristics of mirror-symmetric 7₃-helical poly(di-n-butylsilane) in n-alkanes under static (non-stirring) conditions. In particular, n-dodecane-h₂₆ significantly enhances the circular dichroism (CD) and circularly polarized luminescence (CPL) spectra. A new (−)-CD band emerges at 299 nm below T_C1 ~ 105 °C, with a helix–helix transition at T_C2 ~ 28 °C, and exhibits g_abs = +1.3 × 10⁻² at −10 °C. Synchronously, the CPL band at 340 nm exhibiting g_lum = −0.7 × 10⁻² at 60 °C inverts to g_lum = +2.0 × 10⁻² at 0 °C. Interestingly, clockwise and counterclockwise stirring of the mixture induced non-mirror-image CD spectra. n-Dodecane-d₂₆ weakens the g_abs values by an order of magnitude, and oppositely signed CD and a lower T_C1 of ~45 °C are observed. The notable H/D isotope effect suggests that the CH₃ termini of the polysilane and n-dodecane-h₂₆, which comprise a three identical nuclear spin-1/2 system in a triple-well potential, effectively work as unidirectional hindered rotors due to the handedness of nuclear-spin-dependent parity-violating universal forces. This is supported by the (−)-sign vibrational CD bands in the symmetric and asymmetric bending modes of the CH₃ group in n-dodecane-h₂₆. Full article

A binary Fe₂O₃/Fe₃O₄ mixed nanocomposite was prepared by phyto-mediated avenue to be suited in the photo-Fenton photodegradation of methylene blue (MB) in the presence of H₂O₂. XRD and SEM analyses illustrated that Fe₂O₃ nanoparticles of average crystallite size 8.43 nm were successfully mixed with plate-like aggregates of Fe₃O₄ with a 15.1 nm average crystallite size. Moreover, SEM images showed a porous morphology for the binary Fe₂O₃/Fe₃O₄ mixed nanocomposite that is favorable for a photocatalyst. EDX and elemental mapping showed intense iron and oxygen peaks, confirming composite purity and symmetrical distribution. FTIR analysis displayed the distinct Fe-O assignments. Moreover, the isotherm of the developed nanocomposite showed slit-shaped pores in loose particulates within plate-like aggregates and a mesoporous pore-size distribution. Thermal gravimetric analysis (TGA) indicated the high thermal stability of the prepared Fe₂O₃/Fe₃O₄ binary nanocomposite. The optical properties illustrated a narrowing in the band gab (Eg = 2.92 eV) that enabled considerable absorption in the visible region of solar light. Suiting the developed binary Fe₂O₃/Fe₃O₄ nanocomposite in the photo-Fenton reaction along with H₂O₂ supplied higher productivity of active oxidizing species and accordingly a higher degradation efficacy of MB. The solar-driven photodegradation reactions were conducted and the estimated rate constants were 0.002, 0.0047, and 0.0143 min⁻¹ when using the Fe₂O₃/Fe₃O₄ nanocomposite, pure H₂O₂, and the Fe₂O₃/Fe₃O₄/H₂O₂ hybrid catalyst, respectively. Therefore, suiting the developed binary Fe₂O₃/Fe₃O₄ nanocomposite and H₂O₂ in photo-Fenton reaction supplied higher productivity of active oxidizing species and accordingly a higher degradation efficacy of MB. After being subjected to four photo-Fenton degradation cycles, the Fe₂O₃/Fe₃O₄ nanocomposite catalyst still functioned admirably. Further evaluation of Fe₂O₃/Fe₃O₄ nanocomposite in photocatalytic remediation of contaminated water using a mixture of MB and pyronine Y (PY) dyestuffs revealed substantial dye photodegradation efficiencies. Full article

Non-isocyanate polyurethane (NIPU) networks physically modified with octa(3-hydroxy-3-methylbutyldimethylsiloxy)POSS (8OHPOSS, 0–10 wt%) were conditioned in environments of different relative humidities (up to 97%) to study water–polymer interactions. The equilibrium sorption isotherms are of Brunauer type III in a water activity range of 0–0.97 and are discussed in terms of the Guggenheim (GAB) sorption model. The study shows that the introduction of 8OHPOSS, even in a large amount (10 wt%), does not hinder the water affinity of the NIPU network despite the hydrophobic nature of POSS; this is attributable to the homogenous dispersion of POSS in the polymer matrix. The shift in the urethane-derived carbonyl bands toward lower wavenumbers with a simultaneous shift in the urethane N-H bending bands toward higher wavenumbers exposes the breakage of polymer–polymer hydrogen bonds upon water uptake due to the formation of stronger water–polymer hydrogen bonds. Upon water absorption, a notable decrease in the glass transition temperature ($T_g$) is observed for all studied materials. The progressive reduction in $T_g$ with water uptake is driven by plasticization and slaving mechanisms. POSS moieties are thought to impact slaving indirectly by slightly affecting water uptake at very high hydration levels. Full article

Recently, the pollution of fresh water with heavy metals due to technological and industrial breakthroughs has reached record levels. Therefore, monitoring these metals in fresh water has become essentially urgent. Meanwhile, the conventional periodic one-dimensional phononic crystals can provide a novel platform for detecting the pollution of heavy metals in fresh water with high sensitivity. A simplified design of a defective, one-dimensional phononic crystals (1D-PnC) structure is introduced in this paper. The sensor is designed from a lead-epoxy multilayer with a central defect layer filled with an aqueous solution from cadmium bromide (CdBr₂). The formation of a resonant peak through the transmittance spectrum is highly expected. This study primarily aims to monitor and detect the concentration of cadmium bromide in pure water based on shifting the position of this resonant peak. Notably, any change in cadmium bromide concentration can affect the acoustic properties of cadmium bromide directly. The transfer matrix method has been used to calculate the transmission spectra of the incident acoustic wave. The numerical findings are mainly based on the optimization of the cadmium bromide layer thickness, lead layer thickness, epoxy layer thickness, and the number of periods to investigate the most optimum sensor performance. The introduced sensor in this study has provided a remarkably high sensitivity (S = 1904.25 Hz) within a concentration range of (0–10,000 ppm). The proposed sensor provides a quality factor (QF), a resolution, and a figure of merit of 1398.51752, 48,875,750 Hz, and 4.12088 × 10⁻⁵ (/ppm), respectively. Accordingly, this sensor can be a potentially robust base for a promising platform to detect small concentrations of heavy metal ions in fresh water. Full article